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GlyTouCan
Glycan Structure Repository
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Glycoconjugate Repository
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Glycomics MS raw data Repository
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Glycomics MS Repository for glycan annotations from GlycoWorkbench
LM-GlycoRepo
Repository for lectin-assisted multimodality data
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Genes / Proteins / Lipids Glycans / Glycoconjugates Glycomes Pathways / Interactions / Diseases / Organisms
Alliance of Genome Resources
Alliance of Genome Resources is a gene dataset, which contains curated genome information essential for the understanding of the genetics and genomic basis of human biology, health and disease. All data is retrieved from six major model organism databases and the Gene Ontology including FlyBase, Mouse Genome Database (MGI), Rat Genome Database (RGD), Saccharomyces Genome Database (SGD), WormBase, Zebrafish Information Network (ZFIN), and the GO Consortium. In GlyCosmos, only glycan-related disease information has been extracted from Alliance of Genome Resources.
| Source | Last Updated |
|---|---|
| Alliance of Genome Resources | October 9, 2024 |
| Disease ID | Disease Name | Alliance of Genome Resources ID | Species | Gene ID | Gene Symbol | FlyGlycoDB | Evidence Code Names ▲ | References |
|---|---|---|---|---|---|---|---|---|
| DOID:2747 | glycogen storage disease | HGNC:4707 | Homo sapiens (human) | 2998 | GYS2 |
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| DOID:2030 | anxiety disorder | HGNC:4232 | Homo sapiens (human) | 2668 | GDNF |
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| DOID:0060806 | syndromic X-linked intellectual disability Hedera type | HGNC:18305 | Homo sapiens (human) | 10159 | ATP6AP2 |
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| DOID:0112367 | Coffin-Siris syndrome 8 | HGNC:11105 | Homo sapiens (human) | 6601 | SMARCC2 |
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| DOID:2841 | asthma | HGNC:5331 | Homo sapiens (human) | 64127 | NOD2 |
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| DOID:0110662 | congenital myasthenic syndrome 1B | HGNC:1955 | Homo sapiens (human) | 1134 | CHRNA1 |
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| DOID:1289 | neurodegenerative disease | HGNC:4010 | Homo sapiens (human) | 2521 | FUS |
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| DOID:2018 | hyperinsulinism | HGNC:6081 | Homo sapiens (human) | 3630 | INS |
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| DOID:8483 | retinal artery occlusion | HGNC:3542 | Homo sapiens (human) | 2153 | F5 |
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| DOID:3393 | coronary artery disease | HGNC:603 | Homo sapiens (human) | 338 | APOB |
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| DOID:1245 | vulva cancer | HGNC:4931 | Homo sapiens (human) | 3105 | HLA-A |
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| DOID:11612 | polycystic ovary syndrome | HGNC:644 | Homo sapiens (human) | 367 | AR |
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| DOID:8568 | infectious mononucleosis | HGNC:4948 | Homo sapiens (human) | 3123 | HLA-DRB1 |
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| DOID:0080611 | anterior segment dysgenesis 6 | HGNC:2597 | Homo sapiens (human) | 1545 | CYP1B1 |
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| DOID:11981 | morbid obesity | HGNC:7957 | Homo sapiens (human) | 4887 | NPY2R |
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| DOID:6432 | pulmonary hypertension | HGNC:336 | Homo sapiens (human) | 185 | AGTR1 |
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| DOID:13378 | Kawasaki disease | HGNC:12680 | Homo sapiens (human) | 7422 | VEGFA |
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| DOID:0050717 | methylmalonic aciduria and homocystinuria type cblF | HGNC:23038 | Homo sapiens (human) | 55788 | LMBRD1 |
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| DOID:0111676 | high molecular weight kininogen deficiency | HGNC:6383 | Homo sapiens (human) | 3827 | KNG1 |
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| DOID:936 | brain disease | HGNC:2330 | Homo sapiens (human) | 1376 | CPT2 |
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| DOID:4479 | pseudohypoaldosteronism | HGNC:2553 | Homo sapiens (human) | 8452 | CUL3 |
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| DOID:612 | primary immunodeficiency disease | HGNC:11924 | Homo sapiens (human) | 3604 | TNFRSF9 |
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| DOID:3393 | coronary artery disease | HGNC:983 | Homo sapiens (human) | 590 | BCHE |
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| DOID:0050741 | alcohol dependence | HGNC:4585 | Homo sapiens (human) | 2903 | GRIN2A |
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| DOID:0111431 | essential tremor 4 | HGNC:4010 | Homo sapiens (human) | 2521 | FUS |
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